Method for Sequencing a Polynucelotide Template

ABSTRACT

The invention provides methods for pairwise sequencing of a double-stranded polynucleotide template, which methods result in the sequential determination of nucleotide sequences in two distinct and separate regions of the polynucleotide template.

FIELD OF THE INVENTION

The invention relates to methods for pairwise sequencing of adouble-stranded polynucleotide template, which methods result in thesequential determination of nucleotide sequences in two distinct andseparate regions of the polynucleotide template.

BACKGROUND TO THE INVENTION

Advances in the study of biological molecules have been led, in part, byimprovement in technologies used to characterise the molecules or theirbiological reactions. In particular, the study of the nucleic acids DNAand RNA has benefited from developing technologies used for sequenceanalysis.

U.S. Pat. No. 5,302,509 describes a method for sequencing apolynucleotide template which involves performing multiple extensionreactions using a DNA polymerase or DNA ligase to successivelyincorporate labelled nucleotides or polynucleotides complementary to atemplate strand. In such a “sequencing by synthesis” reaction a newnucleotide strand base-paired to the template strand is built up in the5′ to 3′ direction by successive incorporation of individual nucleotidescomplementary to the template strand. The substrate nucleosidetriphosphates used in the sequencing reaction are blocked to preventover-incorporation and labelled differently, permitting determination ofthe identity of the incorporated nucleotide as successive nucleotidesare added.

In order to carry out accurate sequencing a reversible chain-terminatingstructural modification or “blocking group” may be added to thesubstrate nucleotides to ensure that nucleotides are incorporated one ata time in a controlled manner. As each single nucleotide isincorporated, the blocking group prevents any further nucleotideincorporation into the polynucleotide chain. Once the identity of thelast-incorporated labelled nucleotide has been determined the labelmoiety and blocking group are removed, allowing the next blocked,labelled nucleotide to be incorporated in a subsequent round ofsequencing.

In certain circumstances the amount of sequence data that can bereliably obtained with the use of sequencing-by-synthesis techniques,particularly when using blocked, labelled nucleotides, may be limited.In some circumstances the sequencing “run” may be limited to a number ofbases that permits sequence realignment with the human genome, typicallyaround 25-30 cycles of incorporation. Whilst sequencing runs of thislength are extremely useful, particularly in applications such as, forexample, SNP analysis and genotyping, it would be advantageous in manycircumstances to be able to reliably obtain further sequence data forthe same template molecule.

The technique of “paired-end” or “pairwise” sequencing is generallyknown in the art of molecular biology, particularly in the context ofwhole-genomic shotgun sequencing (Siegel A. F. et al., Genomics. 2000,68: 237-246; Roach J. C. et al., Genomics. 1995, 26: 345-353).Paired-end sequencing allows the determination of two “reads” ofsequence from two places on a single polynucleotide duplex. Theadvantage of the paired-end approach is that there is significantly moreinformation to be gained from sequencing two stretches each of “n” basesfrom a single template than from sequencing “n” bases from each of twoindependent templates in a random fashion. With the use of appropriatesoftware tools for the assembly of sequence information (Millikin S. C.et al., Genome Res. 2003, 13: 81-90; Kent, W. J. et al., Genome Res.2001, 11: 1541-8) it is possible to make use of the knowledge that the“paired-end” sequences are not completely random, but are known to occuron a single duplex, and are therefore linked or paired in the genome.This information has been shown to greatly aid the assembly of wholegenome sequences into a consensus sequence.

Paired-end sequencing has typically been performed by making use ofspecialized circular shotgun cloning vectors known in the art. Aftercutting the vector at a specific single site, the template DNA to besequenced (typically genomic DNA) is inserted into the vector and theends resealed to form a new construct. The vector sequences flanking theinsert DNA include binding sites for sequencing primers which permitsequencing of the insert DNA on opposite strands.

A disadvantage of this approach is that it requires time-consumingcloning of the DNA templates it is desired to sequence into anappropriate sequencing vector. Furthermore, because of the need to clonethe DNA template into a vector in order to position binding sites forsequencing primers at both ends of the template fragment it is extremelydifficult to make use of array-based sequencing techniques. Witharray-based techniques it is generally only possible to sequence fromone end of a nucleotide template, this often being the end proximal tothe point of attachment to the array.

WO 2004/070005 describes a method for double-ended sequencing of apolynucleotide template which can be carried out on a solid support. Themethod relies on simultaneous hybridisation of two or more primers to atarget polynucleotide in a single primer hybridization step. Followingthe hybridization step, all of the primers hybridized to the templateare blocked except for one, which has a free 3′ hydroxyl group whichserves as an initiation point for a first sequencing reaction.Sequencing proceeds until no further chain elongation is possible, orelse the sequencing reaction is terminated. Then one of the blockedprimers is unblocked to give a free 3′ hydroxyl and a second sequencingreaction is performed from this initiation point. Thus, the templateremains intact and attached to the solid support throughout.

A major drawback of this approach based on hybridisation of blocked andunblocked primers is that if it is desired to sequence two regions oncomplementary strands of a double-stranded nucleic acid template then itis necessary to hybridise primers to both complementary strands of thetemplate in a single hybridisation step. Since both strands of thetemplate remain intact and attached to the solid support, hybridisationof the primers to cognate sequences in the template strands willgenerally be unfavourable, against formation of a duplex by annealing ofthe two complementary strands of the template. A further drawback is theneed to ensure the chemical blocking of the first primer to allowsequencing of the second primer. The nature of the non immobilised beadsdescribed in the application means that removal of the primers from thebeads is not straightforward, and thus the sequencing runs are less thanoptimal unless the first primer is completely blocked.

WO 98/44151 and WO 00/18957 both describe methods of nucleic acidamplification which allow amplification products to be immobilised on asolid support in order to form arrays comprised of clusters or“colonies” formed from a plurality of identical immobilisedpolynucleotide strands and a plurality of identical immobilisedcomplementary strands. The nucleic acid molecules present in DNAcolonies on the clustered arrays prepared according to these methods canprovide templates for sequencing reactions, for example as described inWO 98/44152 but to date only a single sequencing read can be obtainedfrom one type of immobilised strand in each colony.

SUMMARY OF THE INVENTION

The present inventors have developed a method for paired-end, orpairwise, sequencing of double-stranded polynucleotide templates,including double-stranded templates present on clustered arrays, such asthose described herein. The term pairwise sequencing refers to a pair ofreads obtained by sequencing two distinct regions, either on the samestrand or the complementary strand of a target polynucleotide duplex.Using the method of the invention it is possible to obtain two linked orpaired reads of sequence information from each double-stranded templateon a clustered array, rather than just a single sequencing read as canbe obtained with prior art methods.

According to the invention there is provided a method for pairwisesequencing of first and second regions of a target double-strandedpolynucleotide, wherein said first and second regions are in the sametarget double-stranded polynucleotide, the method comprising:

(a) providing a solid support having immobilised thereon a plurality ofdouble stranded template polynucleotides each formed from complementaryfirst and second template strands linked to the solid support at their5′ ends;(b) treating the plurality of double stranded template polynucleotidesto denature said double stranded template polynucleotides to facilitatehybridisation of a sequencing primer;(c) hybridising a first sequencing primer to one of the template strandsgenerated in part (b);(d) performing a first sequencing reaction by sequential addition ofnucleotides to the first sequencing primer to generate a first extendedsequencing primer and determine the sequence of a first region of thetarget polynucleotide in the first template strand;(e) removing the first extended sequencing primer from step (d);(f) hybridising a second sequencing primer to one of the templatestrands; and(g) performing a second sequencing reaction by sequential addition ofnucleotides to the second sequencing primer to generate a secondextended sequencing primer and determine the sequence of a second regionof the target polynucleotide, wherein determining the sequences of thefirst and second regions of the target polynucleotide achieves pairwisesequencing of said first and second regions of said targetdouble-stranded polynucleotide.

In one embodiment, both strands of the original polynucleotide duplexremain immobilised, and two primers with different sequences are used togenerate each of the sequencing runs. Steps (b) and (e) may involve athermal or chemical treatment such as 0.1 M sodium hydroxide to denaturethe surface bound double stranded polynucleotides.

In another embodiment, the target double stranded polynucleotide mayalso be prepared such that it contains a region of known sequenceinternal to two regions of unknown sequence. The known sequence maycontain a recognition site for cleavage with a restriction endonuclease.Cleavage with a restriction enzyme would result in two separatepolynucleotides, each immobilised through the 5′-end. The twopolynucleotides may then be subject to denaturing conditions, resultingin two single stranded polynucleotides immobilised through the 5′-end.Each single stranded polynucleotide can be sequenced sequentially togive two separate reads from the one original target

In another embodiment, the target double stranded polynucleotide mayagain be prepared such that it contains a region of known sequenceinternal to two regions of unknown sequence. One end of the immobilisedpolynucleotide may be cleaved from the surface, and the resultingpolynucleotide denatured. The resultant single stranded polynucleotide,anchored via the 5′-end contains two distinct regions able to hybridisea sequencing primer; and two reads may be obtained in sequence.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows a schematic illustration of a paired-end read. In thisprocedure a first oligonucleotide (oligo 1) is hybridised to a templateto be sequenced and used to prime a first sequencing run (run 1, singlebase sequencing SBS through 25 cycles). Oligo 1 is then stripped fromthe template and a second primer (oligo 2) hybridised to a differentregion of the same template and used to prime a second sequencing run(run 2, single base sequencing SBS through 25 cycles). The result is twosequencing reads obtained from different positions within the sametemplate.

FIG. 2 shows results from sequencing reactions on a mixture of fivedifferent template sequences amplified to form clusters.

FIG. 3 shows results from sequencing reactions. The images shown aregenerated from A incorporations. 92% of the run 1 clusters align withrun 2. >99% are detected in run 2.

FIG. 4 shows a schematic of methods for constructing polynucleotidemolecules with known sequence between unknown sequences, whereinrestriction enzymes are used to make ditag sequences(vector-target-target-vector) where the central region between the twoends of the fragment is excised.

FIG. 5 shows a schematic of methods for determining paired reads of longunknown polynucleotide regions without using restriction enzymes.

FIG. 6 shows a schematic of a method for preparing a sample to obtain apaired read from the two ends of a fragment of any length. The methoduses a biotinylated adaptor to isolate circularised inserts comprisingthe adaptor. The circular inserts can then be cleaved and recircularisedusing a further adaptor into circles of smaller size containing twoadaptor regions. The circles can be amplified using primers selectivefor the first adaptor to make a linear template suitable foramplification.

FIG. 7 shows a schematic of a method for preparing a sample to obtain apaired read from the two ends of a fragment of any length. The methoduses a biotinylated adaptor to isolate circularised inserts containingthe adaptor, the circles then being fragmented and treated such that theends also comprise adaptors that allow subsequent amplification andsequencing.

FIG. 8 shows a schematic of the method of the invention wherein thecentral known region comprises a site for a particular restrictionenzyme. Upon treatment with the restriction enzyme, two sequencing readscan be obtained from the central region of the amplified fragments. Morespecifically, one read can be obtained from each strand of theimmobilised duplex.

FIG. 9 shows a schematic for the preparation of a sample suitable forobtaining a pair of reads of a fragment of any length. The method isbased on amplifying the fragments with a controlled amount of dUTP,thereby introducing a low level of modifications that allow thefragments to be randomly cut (i.e. cut where a uracil base is randomlyinserted). The cut fragments can be religated into circles and amplifiedsuch that the two ends of the original PCR fragments are joined togetherwith the central bases excised.

FIG. 10 shows a schematic for the preparation of a sample suitable forobtaining a pair of reads of a fragment of any length. The method isbased on oxidising the guanine bases to a low level in the originalsample, thereby introducing a low level of modifications that allow thefragments to be randomly cut (i.e. cut where a guanine base is randomlyoxidised). The cut fragments can be religated into circles and amplifiedsuch that the two ends of the original PCR fragments are joined togetherwith the central bases excised.

FIG. 11 shows a schematic for the preparation of a sample suitable forobtaining a pair of reads of a fragment of any length. The method isbased on oxidising the guanine bases to a low level in the originalsample, thereby introducing a low level of modifications that allow thefragments to be randomly cut (i.e. cut where a guanine base is randomlyoxidised). If the vector-target ligated circles are cut open using anenzyme that removes the 8-oxo guanine bases, then only the ends of thetarget fragments remain attached to the vector. A new adaptor sequencecan be attached to reclose the polished ends, producing a fragment withtwo known ends from the original vector, two ends from a target fragmentand a central adaptor sequence. The fragment can be linearized byamplification using primers complementary to the ends of the originalvector.

FIG. 12 shows the structure and sequence of an exemplary double strandedDNA template used for solid phase amplification in the accompanyingexamples. Sequences of the amplification primers P5 and P7 are shown inbold type.

DETAILED DESCRIPTION OF THE INVENTION

The invention provides methods for sequencing two regions of a targetdouble-stranded polynucleotide template, referred to herein as the firstand second regions for sequence determination. The first and secondregions for sequence determination are either on the same strand, or oncomplementary strands, of the double-stranded polynucleotide template,which are referred to herein respectively as first and second templatestrands.

The starting point for the method of the invention is the provision of aplurality of template polynucleotide duplexes immobilised on a solidsupport in the form of amplified clusters as described in WO9844151 andWO00018957, whose contents are incorporated herein by reference. Each ofthe duplexes within a particular cluster comprises the samedouble-stranded target region to be sequenced. The duplexes are eachformed from complementary first and second template strands which arelinked to the solid support at or near to their 5′ ends. Typically, thetemplate polynucleotide duplexes will be provided in the form of aclustered array.

WO07010252 also describes a method of reading both the first and secondtemplate strands from each cluster, but suffers from the disadvantagethat only half the strands in each cluster are sequenced. Thisdiminishes the signal intensity of the sequencing reads. The methodologydescribed herein allows the sequencing of essentially all of the copiesof each strand in each cluster, and therefore produces a signal ofgreater intensity than the previous methodology. This property of thepresent methodology confers greater sensitivity with respect to signaldetection and means that longer reads can be obtained from smallerclusters than the prior art.

When referring to immobilisation or attachment of molecules (e.g.nucleic acids) to a solid support, the terms “immobilised” and“attached” are used interchangeably herein and both terms are intendedto encompass direct or indirect, covalent or non-covalent attachment,unless indicated otherwise, either explicitly or by context. In certainembodiments of the invention covalent attachment may be preferred, butgenerally all that is required is that the molecules (e.g. nucleicacids) remain immobilised or attached to the support under theconditions in which it is intended to use the support, for example inapplications requiring nucleic acid amplification and/or sequencing.

Certain embodiments of the invention may make use of solid supportscomprised of an inert substrate or matrix (e.g. glass slides, polymerbeads etc) which is been “functionalised”, for example by application ofa layer or coating of an intermediate material comprising reactivegroups which permit covalent attachment to biomolecules, such aspolynucleotides. Examples of such supports include, but are not limitedto, polyacrylamide hydrogels supported on an inert substrate such asglass. In such embodiments, the biomolecules (e.g. polynucleotides) maybe directly covalently attached to the intermediate material (e.g. thehydrogel) but the intermediate material may itself be non-covalentlyattached to the substrate or matrix (e.g. the glass substrate). The term“covalent attachment to a solid support” is to be interpretedaccordingly as encompassing this type of arrangement.

As will be apparent to the skilled reader, references herein to aparticular nucleic acid sequence may, depending on the context, alsorefer to nucleic acid molecules which comprise the nucleic acidsequence. Sequencing of a target fragment means that a read of thechronological order of bases is established. The bases do not, however,need to be contiguous, nor does every base on the entire fragment haveto be sequenced.

The following passages describe different aspects of the invention ingreater detail. Each aspect of the invention may be combined with anyother aspect or aspects of the invention unless clearly indicated to thecontrary. In particular, any feature indicated as being particular,preferred or advantageous may be combined with any other feature orfeatures indicated as being particular, preferred or advantageous.

The terms ‘target nucleic acid sequence’, ‘target nucleic acidmolecule’, ‘target nucleic acid’ and ‘target nucleic acid fragment’ maybe used interchangeably to refer to nucleic acid molecules that it isdesired to sequence on an array according to the invention. The targetnucleic acid may be essentially any nucleic acid of known or unknownsequence. It may be, for example, a fragment of genomic DNA or cDNA.Sequencing may result in determination of the sequence of the whole, ora part of the target molecule. The targets can be derived from a primarynucleic acid sample that has been randomly fragmented. The targets canbe processed into templates suitable for amplification by the placementof universal amplification sequences at the ends of each targetfragment. The targets can also be obtained from a primary RNA sample byreverse transcription into cDNA.

As used herein, the term ‘polynucleotide’ refers to deoxyribonucleicacid (DNA), but where appropriate the skilled artisan will recognisethat the method may also be applied to ribonucleic acid (RNA). The termsshould be understood to include, as equivalents, analogs of either DNAor RNA made from nucleotide analogs and to be applicable to singlestranded (such as sense or antisense) and double strandedpolynucleotides. The term as used herein also encompasses cDNA, that iscomplementary or copy DNA produced from an RNA template, for example bythe action of reverse transcriptase.

The primary polynucleotide molecules may originate in double-strandedDNA (dsDNA) form (e.g. genomic DNA fragments, PCR and amplificationproducts and the like) or may have originated in single-stranded form,as DNA or RNA, and been converted to dsDNA form. By way of example, mRNAmolecules may be copied into double-stranded cDNAs suitable for use inthe method of the invention using standard techniques well known in theart. The precise sequence of the primary polynucleotide molecules isgenerally not material to the invention, and may be known or unknown.

In a particular embodiment, the primary polynucleotide molecules are DNAmolecules. More particularly, the primary polynucleotide moleculesrepresent the entire genetic complement of an organism, and are genomicDNA molecules which include both intron and exon sequences (codingsequence), as well as non-coding regulatory sequences such as promoterand enhancer sequences. In an embodiment wherein genomic DNA moleculesare used, genome-wide analysis or analysis of the entire genome may beachieved. It is, however, envisaged that particular sub-sets ofpolynucleotide sequences or genomic DNA could also be used, such as, forexample, particular chromosomes. Yet more particularly, the sequence ofthe primary polynucleotide molecules is not known. Still yet moreparticularly, the primary polynucleotide molecules are human genomic DNAmolecules. The DNA target molecules may be treated chemically orenzymatically, either prior to, or subsequent to any randomfragmentation processes, and prior to or subsequent to the ligation ofthe adaptor sequences.

Random fragmentation refers to the fragmentation of a polynucleotidemolecule in a non-ordered fashion by enzymatic, chemical or mechanicalmeans. Such fragmentation methods are known in the art and utilisestandard methods (Sambrook and Russell, Molecular Cloning, A LaboratoryManual, third edition). For the sake of clarity, generating smallerfragments of a larger piece of nucleic acid via specific PCRamplification of such smaller fragments is not equivalent to fragmentingthe larger piece of nucleic acid because the larger piece of nucleicacid sequence remains in intact (i.e., is not fragmented by the PCRamplification). Moreover, random fragmentation is designed to producefragments irrespective of the sequence identity or position ofnucleotides comprising and/or surrounding the break. More particularly,random fragmentation is achieved by mechanical means such asnebulisation or sonication and produces fragments of about 50 base pairsin length to about 1500 base pairs in length, still more particularly50-700 base pairs in length, yet more particularly 50-400 base pairs inlength. Most particularly, the method is used to generate smallerfragments of from 50-150 base pairs in length.

Fragmentation of polynucleotide molecules by mechanical means(nebulization, sonication and Hydroshear for example) results infragments with a heterogeneous mix of blunt and 3′- and 5′-overhangingends. It is therefore desirable to repair the fragment ends usingmethods or kits (such as the Lucigen DNA terminator End Repair Kit)known in the art to generate ends that are optimal for insertion, forexample, into blunt sites of cloning vectors. In a particularembodiment, the fragment ends of the population of nucleic acids areblunt ended. More particularly, the fragment ends are blunt ended andphosphorylated. The phosphate moiety can be introduced via enzymatictreatment, for example, using polynucleotide kinase.

In a particular embodiment, the target polynucleotide sequences areprepared with single overhanging nucleotides by, for example, activityof certain types of DNA polymerase such as Taq polymerase or Klenow exominus polymerase which has a nontemplate-dependent terminal transferaseactivity that adds a single deoxynucleotide, for example, deoxyadenosine(A) to the 3′ ends of, for example, PCR products. Such enzymes can beutilised to add a single nucleotide ‘A’ to the blunt ended 3′ terminusof each strand of the target polynucleotide duplexes. Thus, an ‘A’ couldbe added to the 3′ terminus of each end repaired duplex strand of thetarget polynucleotide duplex by reaction with Taq or Klenow exo minuspolymerase, whilst the adaptor polynucleotide construct could be aT-construct with a compatible ‘T’ overhang present on the 3′ terminus ofeach duplex region of the adaptor construct. This end modification alsoprevents self-ligation of both vector and target such that there is abias towards formation of the combined ligated adaptor-target sequences.

Paired reads can be obtained on fragments of any length, for example PCRamplicons of 2-10 Kb or DNA clones isolated from bacteria or otherbiological sources. The targets may be the ends of phosmid molecules ofaround 40 kB or the ends of Bacterial artificial chromosomes (BAC's) ofaround 100-200 kB. The ends of targets derived from such sources may besequenced without fragmentation to obtain the reads from the ends ofeach unfragmented target, or the target may be fragmented. Thefragmented targets may be size selected, for example by gelelectrophoresis, to obtain a narrow size distribution on the targetfragments. Paired reads spaced throughout the sample may be used as atool for de-novo assembly of a previously unsequenced sample, as well asfor resequencing a sample where a reference genome is available. Themethods described herein are suitable for use with nucleic acidmolecules obtained from any source, where knowledge of the sequences ateither end of the molecules is desired.

In order to sequence two regions of a given target double-strandedpolynucleotide using the method of the invention, it is necessary tocarry out sequential sequencing reactions. To enable two separatesequencing reactions it is in turn necessary to sequentially hybridiseto two different single-stranded regions to serve as templates forsequencing. Formation of suitable single-stranded regions for sequencingcan be achieved by any of the ways described herein.

Sequential Hybridisation

The immobilised duplex contains two complementary strands, eachimmobilised through the 5′-end to the surface. Denaturing the doublestranded polynucleotide results in two single stranded polynucleotides;each capable of hybridising a different sequencing primer. Using a firstsequencing primer complementary to the 3′-end of one of the boundstrands, allows a sequencing read to be obtained from one of thestrands. This sequencing run can then be denatured; and a second primercomplementary to the 3′-end of the other strand can be hybridised. Thesequencing protocol can then be repeated to obtain a second run; at theopposite end of the polynucleotide molecule of the first run.

The denaturing treatment used to denature the immobilisedpolynucleotide, or remove the first sequencing primer can be heat to atemperature in excess of 95° C., or a chemical treatment with adenaturing solution such as 0.1 M sodium hydroxide; 50% formamide or 8 Murea solution.

The sequencing primers can remain immobilised during the first andsecond reads. If the double stranded polynucleotide is designed tocontain a sequence selective nicking site on each strand, the sequencingreads can be performed sequentially, using the 3′ side of the nickedstrand as an initiation point, after each strand is nicked. The 5-end ofthe nicked strand remains immobilised, and can be blocked after thefirst sequencing run, before treatment to nick the second strand isperformed. In this case the duplex is not denatured to allowhybridisation of a sequencing primer, but the first strand is nicked toallow a part of the original duplex to function as a sequencing primerand sequence the second strand. The second read is commenced by a nickof the second strand of the duplex, allowing the read of the firststrand. In this embodiment, it is important not to subject the array todenaturing conditions at any point, since during the second read, thetemplate is only attached to the surface by hybridisation.

Cluster Cleavage Using a Restriction Endonuclease

The double stranded polynucleotide templates comprise sequences ofunknown target DNA between known adaptors at the ends of the sequences.However, it is straightforward to use molecular biology techniques toconstruct a polynucleotide where there is also a known region ofnucleotide sequence splitting the unknown region in two. The templatepolynucleotide can thus be represented as having a known end, a stretchof unknown sequence, a known adaptor region, another unknown sequence,and a known second end, herein defined asadaptor-target-adaptor-target-adaptor constructs if they are not furtheramplified, or primer-target-adaptor-target-primer if the initialadaptor-target-adaptor-target-adaptors are subject to amplification. Theinternal sequences can be designed to contain two sequencing primersites; as well as a site that allows sequence selective cutting of bothstrands of the duplex, for example a restriction endonucleaserecognition site, as shown in FIG. 8. Such restriction endonuclease cutsgive two anchored polynucleotide duplexes immobilised at the 5′ end ofone of the strands. The immobilised duplexes can be denatured by heatingor chemical treatment, resulting in two non-complementary singlestranded polynucleotides immobilised in close proximity. Each of thesenon complementary strands can be sequenced using different sequencingprimers to give two reads derived from the original polynucleotideduplex.

Construction of the double stranded polynucleotide templates with aninternal primer region can be performed by ligating the randomisedgenomic fragments into a linearised vector to re-make the circularconstruct. Cutting away from the known sections of the circularisedvector into the unknown region using remote cutting restriction enzymessuch as MmeI or EcoP15, allows the central region of the unknownsequences to be removed. EcoP15I is a type III restriction enzyme thatrecognizes the sequence motif CAGCAG and cleaves the double stranded DNAmolecule 27 base pairs downstream of the CAGCAG motif. The cut sitecontains a 2 base 5′-overhang that can be end repaired to give a 27 baseblunt ended duplex. Under normal in vivo conditions EcoP15I requires twoCAGCAG motifs oriented in a head to head orientation on opposite strandsof the double stranded molecule, and then the enzyme cleaves the duplexat only one of the two sites. However, under specific in vitroconditions in the presence of the antibiotic compound sinefungin (Sigmacat number S8559) EcoP15I has the desired effect of inducing cleavage ofa double stranded duplex at all CAGCAG sequences present in a sequenceirrespective of number or orientation, as shown by Raghavendra & Rao(Biochem Biophys Res Commun. 2005 Sep. 2; 334 (3):803-11), which isincorporated herein in its entirety, however to the best of ourknowledge, the use of sinefungin, or an analogue thereof in thepreparation of ditag libraries using EcoP15 or other type IIIrestriction endonucleases is previously unreported.

The ends of each molecule can either be joined back together to make asingle nucleotide ‘ditag’ sequence of type vector-target-target-vector,or an adaptor of known sequence can be used to act as a spacer region ina template of type vector-target-adaptor-target-vector, as shown in FIG.4. An alternative way of building this type of construct is to open acircularised vector molecule and ligate adaptors onto each end, anexample of which is shown in FIG. 7 where the fragmentation can be bythe remote cutting restriction enzyme rather than the randomised methodalso covered in FIG. 7.

In the preparation of DNA templates for cluster production and SBS, twoEcoP15I sites and other known adaptor sequences were attached to acircular vector with the target sequence in close proximity to theunknown target sequence, as shown in FIG. 4. The proximity of theEcoP151 sites to the target sequence allows cleavage at a specificposition 27 bp into the target sequence, thus allowing manipulation of27 base sequences of the unknown target sequence. The use of two EcoP15Isites at either end of the target DNA fragment, allows the removal ofthe majority of the target sequence leaving two associated 27 bpfragments at either end. A single sequencing read of 54 bases givessequence information from the two ends of the original target, withoutthe intervening bases. The construct of 54 contiguous bases is anexample of a ditag, as it comprises the two 27 base pair ends of theoriginal target connected together. This Ecop15 specific ditag constructcomprises vector-target (27 bases)-target (27 bases)-vector. If thecircular ditags are amplified with primers complementary to the vectorregions, a linear ditag construct primer-target (27bases)-target (27bases)-primer is obtained.

Religation to close a circular construct can be accomplished usingsequences of any length sufficient to ensure efficient closure of thecircle. Amplification using primers on either side of the original cutsite will give copies of the desired polynucleotide template. However,the length of the unknown region that can be generated using such di-tagmethods is limited by the availability of remote cutting restrictionenzymes. Examples of the construction of such a library usingrestriction enzymes have been reported (Science 2005; Vol. 309. no.5741, pp. 1728-1732).

Methods of producing ditags are well documented in, for example,WO00179553, WO03074734, WO06135342 or US2006/0024681. The amplificationof single molecules of such ditags to produce a clustered array whereinboth strands of each amplified duplex are immobilised, as taught for thefirst time by the present inventors, confers a significant advantage inthat it is possible to simultaneously analyse a large number of ditagsof different sequences on a single solid support. Moreover, inserting anadaptor into the ditag allows four sequencing reads from each templateduplex rather than just two reads. Another significant limitation ofprior art methods is the requirement to use restriction enzymes, whichlimit the length of the target sequences. The methods detailed hereinwhich do not require the use of restriction enzymes provide asignificant advantage in terms of the length of the two target fragmentsthat can be sequenced.

An alternative approach with which to generate the desired constructswherein the target polynucleotide fragments are longer than arestriction enzyme cut site, which are of particular advantage in thecurrent invention, is to ligate a linear adaptor sequence into theunknown fragments to form a circular construct. A random shearingprocess such as sonication, nebulisation or exonuclease treatment canthen be used to generate linear constructs containing a central adaptorsequence. The adaptors may be modified with groups such as biotin to aidpurification of the adaptor-target circles or their fragments. Endrepair, followed by circularisation with another adaptor will generate acircular product with two known and two unknown regions. This can beamplified using pairs of primers to generate the desiredknown-unknown-known-unknown-known polynucleotide template. There are anumber of variations on this technique, and the order of the steps isnot fixed. It is anticipated that any technique used to generate apolynucleotide molecule containing known ends, and a known internalsequence between two unknown regions of interest for sequencing isencompassed within the scope of the current invention. A variety ofmethods that may be applicable to this type of sample preparationtechnique are shown in FIGS. 5, 6, 7, 9, 10 and 11. These methods aredescribed below in reference to the figures.

FIG. 5 shows a schematic of methods for determining paired reads of longunknown polynucleotide regions without using restriction enzymes. Thetarget inserts, can be, for example: PCR amplicons, randomly shearednucleic acid samples isolated from biological samples (for examplebacteria, viruses or other organisms), isolated clones, libraries ofclones, plasmids, phosmids or any other source of nucleic acid that canbe ligated into circles using suitable adaptors. The randomly shearedtargets may be end repaired prior to ligation. If the sample isfragmented prior to ligation, then the fragments may be size selectedinto narrow distributions prior to ligation, or the fragmentation may becontrolled to achieve fragments of a narrow size distribution atound acertain size, for example, 5 kb or 10 kb.

The circular constructs may be randomly fragmented, again using avariety of techniques such as sonication, nebulisation or hydroshearing.Due to the random nature of these processes, the fragments will be amixture of those fragments that contain the adaptor sequence and thosethat do not. The fragmentation process may be less random if the adaptoris protected from fragmentation. Since the sequence of the adaptorregion is known, this sequence may be used to selectively target DNAbinding proteins or similar reagents to the adaptor region. If theproteins are of sufficient size, they will also bind the target sequenceand protect the target from further fragmentation. The proteins could betargeted using the known sequence of the adaptor regions, for exampleusing oligonucleotide-protein conjugates. It may be advantageous in suchinstances to use triplex forming oligonucleotides or molecules that canhybridise strongly to a duplex, such as peptide nucleic acid (PNA), thatcan strand invade into the duplex.

Suitable DNA binding proteins might include transcription factors, DNApolymerases or other nucleic acid modifying enzymes, chromatin orrestriction enzymes, where the site of binding has been modified suchthat a cut is not possible. The size of the area protected depends onthe method used to protect the target sequence, but may be from 20-200bases from each end of the adaptor sequence.

The fragments can be re-circularised using a second adaptor to obtainessentially two types of circular constructs, those with only the secondadaptor and those with both the first and second adaptors. Amplificationof the circles with primers specific for the first adaptor will resultin amplification of only those circles that contain the intact firstadaptor sequence, and therefore only the desired products containing theconstruct primer-target-adaptor-target-primer will be obtained.

In all examples where circles are amplified, the amplification methodmay involve two primers as a standard amplification reaction, or may beperformed by rolling circle amplification. In some instances two primersmay be used in rolling circle amplification methods such that theintital copies of the circular templates are further amplified.

FIG. 6 shows a variation on FIG. 5 wherein the initial adaptors arebiotinylated. Biotinylation of the adaptors allows some or all of thesteps to be carried out on a solid support, or to purify the desiredfragments when required. If the adaptors are ligated to the targets asdescribed above, the non ligated target will not carry a biotinmodification, so it can be readily removed from the mixture ofmolecules. Once the circles are fragmented, again the biotin group onthe adaptor allows selection of the fragments that carry the initialadaptor over those that do not. The adaptor containing fragments can beligated with a second adaptor as described above, and amplified withprimers specific for the first adaptor sequence to make a lineartemplate suitable for further amplification and/or sequencing.

FIG. 7 shows a variation on FIG. 6 wherein the fragmented circles aretreated with adaptors such that both ends of the linear fragments aremodified. This circumvents the need for a second circularisationreaction, whilst still allowing preparation of a construct of typeadaptor-target-adaptor-target-adaptor.

FIG. 9 shows a schematic for the preparation of a sample for obtaining apair of reads from the distal ends of a fragment of any length. Themethod is based on amplifying the fragments with a controlled amount ofdUTP, thereby introducing a low level of modifications that allow thefragments to be randomly cut (i.e. cut where a uracil base is randomlyinserted). The cut fragments can be religated into circles and amplifiedsuch that the two ends of the original PCR fragments are joined togetherwith the central bases excised.

FIG. 10 shows a schematic for the preparation of a sample suitable forobtaining a pair of reads from the distal ends of a fragment of anylength, without the need for an initial PCR reaction to introduce themodified bases needed for subsequent cleavage. The method is based onoxidising the guanine bases to a low level in the original sample,thereby introducing a low level of modifications that allow thefragments to be randomly cut (i.e. cut where a guanine base is randomlyoxidised). The cut fragments can be religated into circles and amplifiedsuch that the two ends of the original PCR fragments are joined togetherwith the central bases excised.

FIG. 11 shows a schematic for the preparation of a sample suitable forobtaining a pair of reads from the distal ends of a fragment of anylength. The method is based on oxidising the guanine bases to a lowlevel in the original sample, thereby introducing a low level ofmodifications that allow the fragments to be randomly cut (i.e. cutwhere a guanine base is randomly oxidised). If the vector-target ligatedcircles are cut open using an enzyme that removes the 8-oxo guaninebases, then only the ends of the target fragments will remain attachedto the vector. A new adaptor sequence can be attached to re-circularizethe polished ends, producing a fragment with two known ends from theoriginal vector, two ends from a target fragment and a central adaptorsequence. The fragment can be linearized by amplification using primerscomplementary to the ends of the original vector to give aprimer-target-adaptor-target-primer construct suitable for furtheramplification and/or sequencing.

Linearisation of Immobilised DNA

Polynucleotide molecules can be prepared to contain sequences for twosequencing primers as described above. If such molecules are immobilisedsuch that one of the two immobilised ends can be cleaved from thesurface, upon such cleavage the resulting double stranded DNA, which isnow immobilised at only one end of the duplex, can be made singlestranded using heat or chemical denaturing conditions to give a singlestranded molecule containing two primer hybridisation sites. The processof removing all or a portion of one immobilised strand in a ‘bridged’double-stranded nucleic acid structure may be referred to herein as‘linearisation’. The single stranded molecule can be sequenced using afirst sequencing primer, which can then be removed and a secondsequencing primer introduced to allow a second read. If the constructsare not linearised, then it is possible to obtain four reads from eachduplex, since each strand can be sequenced twice, once from the 3′terminal adaptor sequence, and once from the central adaptor sequence.

To linearise the immobilised duplex strands, either the first or secondstrand of the template duplexes must include a cleavage site. Saidcleavage site is a site which allows controlled cleavage of the first orsecond template strand by chemical, enzymatic or photochemical means.The double stranded polynucleotide is then only immobilised through oneend. The polynucleotide is then denatured to leave a single strandedpolynucleotide immobilised at the 5′-end. A first sequencing primer canthen be hybridised to a single-stranded region of the template and usedas the primer for a sequencing reaction, after which it is removed fromthe template, and a second sequencing primer is hybridised and used forsequencing of a different region of the single stranded template.

Any suitable enzymatic, chemical or photochemical cleavage reaction maybe used to cleave. The cleavage reaction may result in removal of a partor the whole of the strand being cleaved. Suitable cleavage meansinclude, for example, restriction enzyme digestion, in which case thecleavage site is an appropriate restriction site for the enzyme whichdirects cleavage of one or both strands of a duplex template; RNasedigestion or chemical cleavage of a bond between a deoxyribonucleotideand a ribonucleotide, in which case the cleavage site may include one ormore ribonucleotides; chemical reduction of a disulphide linkage with areducing agent (e.g. TCEP), in which case the cleavage site shouldinclude an appropriate disulphide linkage; chemical cleavage of a diollinkage with periodate, in which case the cleavage site should include adiol linkage; generation of an abasic site and subsequent hydrolysis,etc.

In one embodiment cleavage may occur at a cleavage site in one or bothstrands of a template polynucleotide duplex which comprises one or moreor any combination of non-natural nucleotides, ribonucleotides or anon-nucleotide chemical modifications.

Suitable cleavage techniques for use in the method of the invention aredescribed in full in co-pending application WO07010251, and include, butare not limited to, the following:

i) Chemical Cleavage

The term “chemical cleavage” encompasses any method which utilises anon-nucleic acid and non-enzymatic chemical reagent in order topromote/achieve cleavage of one or both strands of a templatepolynucleotide duplex. If required, one or both strands of the templatepolynucleotide duplex may include one or more non-nucleotide chemicalmoieties and/or non-natural nucleotides and/or non-natural backbonelinkages in order to permit chemical cleavage reaction. In a particularembodiment, the modification(s) required to permit chemical cleavage maybe incorporated into an amplification primer used to form the templatepolynucleotide duplex by solid-phase nucleic acid amplification.

In a particular embodiment, one strand of the template polynucleotideduplex (or the amplification primer from which this strand is derived ifformed by solid-phase amplification) may include a diol linkage whichpermits cleavage by treatment with periodate (e.g. sodium periodate). Itwill be appreciated that more than one diol can be included at thecleavage site.

Diol linker units based on phosphoamidite chemistry suitable forincorporation into polynucleotide chains are commercially available fromFidelity systems Inc. (Gaithersburg, Md., USA) or can be chemicallyprepared as described in WO07010251. One or more diol units may beincorporated into a polynucleotide using standard methods for automatedchemical DNA synthesis. Hence, oligonucleotide primers including one ormore diol linkers can be conveniently prepared by chemical synthesis.

In order to position the diol linker at an optimum distance from thesolid support one or more spacer molecules may be included between thediol linker and the site of attachment to the solid support. Tofacilitate attachment to a solid support at the 5′ end of thepolynucleotide strand, the 5′ end may be modified to include aphosphorothioate group. The phosphorothioate group can easily beattached during chemical synthesis of a “polynucleotide” chain includingthe spacer and diol units. The spacer molecules may include, forexample, a stretch of nucleotides that are not complementary to thetemplates being amplified. Typically from 1 to 20, more particularlyfrom 1 to 15 or from 1 to 10, and even more particularly 2, 3, 4, 5, 6,7, 8, 9 or 10 spacer nucleotides may be included. In a particularembodiment, 10 spacer nucleotides are positioned between the point ofattachment to the solid support and the diol linker. In anotherparticular embodiment, polyT spacers are used, although othernucleotides and combinations thereof can be used. In another particularembodiment, the primer may include 10T spacer nucleotides.

The diol linker is cleaved by treatment with a “cleaving agent”, whichcan be any substance which promotes cleavage of the diol. One suchcleaving agent is periodate, for example aqueous sodium periodate(NaIO₄). Following treatment with the cleaving agent (e.g. periodate) tocleave the diol, the cleaved product may be treated with a “cappingagent” in order to neutralise reactive species generated in the cleavagereaction. Suitable capping agents for this purpose include amines, suchas ethanolamine or propanolamine (3-amino-propan-l-ol). Advantageously,the capping agent (e.g. propanolamine) may be included in a mixture withthe cleaving agent (e.g. periodate) so that reactive species are cappedas soon as they are formed.

The example of a combination of a diol linkage and cleaving agent (e.g.periodate) to achieve cleavage of at least one strand of a templatepolynucleotide duplex works well for linearisation of template duplexeson solid supported polyacrylamide hydrogels as treatment with periodateand propanolamine is compatible with nucleic acid integrity and with thechemistry of the hydrogel surface. Utility of diol linkages/periodate asa method of linearisation is not, however, limited to polyacrylamidehydrogel surfaces but also extends to linearisation of duplexesimmobilised on other solid supports and surfaces, including supportscoated with functionalised silanes (etc).

In a further embodiment, the strand to be cleaved (or the amplificationprimer from which this strand is derived if prepared by solid-phaseamplification) may include a disulphide group which permits cleavagewith a chemical reducing agent, e.g. Tris (2-carboxyethyl)-phosphatehydrochloride (TCEP).

ii) Cleavage of Abasic Sites

An “abasic site” is defined as a nucleotide position in a polynucleotidechain from which the base component has been removed. Abasic sites canoccur naturally in DNA under physiological conditions by hydrolysis ofnucleotide residues, but may also be formed chemically under artificialconditions or by the action of enzymes. Once formed, abasic sites may becleaved (e.g. by treatment with an endonuclease or other single-strandedcleaving enzyme, exposure to heat or alkali), providing a means forsite-specific cleavage of a polynucleotide strand.

In a particular, but non-limiting embodiment, an abasic site may becreated at a pre-determined position on one strand of a templatepolynucleotide duplex and then cleaved by first incorporatingdeoxyuridine (U) at a pre-determined cleavage site in one strand of thetemplate polynucleotide duplex. This can be achieved, for example, byincluding U in one of the primers used for preparation of the templatepolynucleotide duplex by solid-phase PCR amplification. The enzymeuracil DNA glycosylase (UDG) may then be used to remove the uracil base,generating an abasic site on one strand. The polynucleotide strandincluding the abasic site may then be cleaved at the abasic site bytreatment with endonuclease (e.g EndoIV endonuclease, AP lyase, FPGglycosylase/AP lyase, EndoVIII glycosylase/AP lyase), heat or alkali.

Abasic sites may also be generated at non-natural/modifieddeoxyribonucleotides other than deoxyuridine and cleaved in an analogousmanner by treatment with endonuclease, heat or alkali. For example,8-oxo-guanine can be converted to an abasic site by exposure to FPGglycosylase. Deoxyinosine can be converted to an abasic site by exposureto AlkA glycosylase. The abasic sites thus generated may then becleaved, typically by treatment with a suitable endonuclease (e.g.EndoIV, AP lyase). If the non-natural/modified nucleotide is to beincorporated into an amplification primer for use in solid-phaseamplification, then the non-natural/modified nucleotide should becapable of being copied by the polymerase used for the amplificationreaction.

In one embodiment, the molecules to be cleaved may be exposed to amixture containing the appropriate glycosylase and one or more suitableendonucleases. In such mixtures the glycosylase and the endonucleasewill typically be present in an activity ratio of at least about 2:1.

This method of cleavage has particular advantages in relation to thecreation of templates for nucleic acid sequencing. In particular,cleavage at an abasic site generated by treatment with a glycosylasesuch as UDG generates a free 3′ hydroxyl group on the cleaved strandwhich can provide an initiation point for sequencing a region of thecomplementary strand. Moreover, if the initial double-stranded nucleicacid contains only one cleavable (e.g. uracil) base on one strand then asingle “nick” can be generated at a unique position in this strand ofthe duplex. Since the cleavage reaction requires a residue, e.g.deoxyuridine, which does not occur naturally in DNA, but is otherwiseindependent of sequence context, if only one non-natural base isincluded there is no possibility of glycosylase-mediated cleavageoccurring elsewhere at unwanted positions in the duplex. In contrast,were the double-stranded nucleic acid to be cleaved with a “nicking”endonuclease that recognises a specific sequence, there is a possibilitythat the enzyme may create nicks at “other” sites in the duplex (inaddition to the desired cleavage site) if these possess the correctrecognition sequence. This could present a problem if nicks are createdin the strand it is intended to sequence rather than the strand thatwill be fully or partially removed to create the sequencing template andis a particular risk if the target portion of the double-strandednucleic acid molecule is of unknown sequence.

The fact that there is no requirement for the non-natural (e.g. uracil)residue to be located in a detailed sequence context in order to providea site for cleavage using this approach is itself advantageous. Inparticular, if the cleavage site is to be incorporated into anamplification primer to be used in the production of a clustered arrayby solid-phase amplification, it is necessarily only to replace onenatural nucleotide (e.g. T) in the primer with a non-natural nucleotide(e.g. U) in order to enable cleavage. There is no need to engineer theprimer to include a restriction enzyme recognition sequence of severalnucleotides in length. Oligonucleotide primers including U nucleotides,and other non-natural nucleotides, such as those listed above, caneasily be prepared using conventional techniques and apparatus forchemical synthesis of oligonucleotides.

Another advantage gained by cleavage of abasic sites in adouble-stranded molecule generated by action of UDG on uracil is thatthe first base incorporated in a “sequencing-by-synthesis” reactioninitiating at the free 3′ hydroxyl group formed by cleavage at such asite will always be T. Hence, if the template polynucleotide duplexforms part of a clustered array comprised of many such molecules, all ofwhich are cleaved in this manner to produce sequencing templates, thenthe first base universally incorporated across the whole array will beT. This can provide a sequence-independent assay for individual clusterintensity at the start of a sequencing “run”.

iii) Cleavage of Ribonucleotides

Incorporation of one or more ribonucleotides into a polynucleotidestrand which is otherwise comprised of deoxyribonucleotides (with orwithout additional non-nucleotide chemical moieties, non-natural basesor non-natural backbone linkages) can provide a site for cleavage usinga chemical agent capable of selectively cleaving the phosphodiester bondbetween a deoxyribonucleotide and a ribonucleotide or using aribonuclease (RNAse). Therefore, sequencing templates can be produced bycleavage of one strand of a template polynucleotide duplex at a sitecontaining one or more consecutive ribonucleotides using such a chemicalcleavage agent or an RNase. Particularly, the strand to be cleavedcontains a single ribonucleotide to provide a site for chemicalcleavage.

Suitable chemical cleavage agents capable of selectively cleaving thephosphodiester bond between a deoxyribonucleotide and a ribonucleotideinclude metal ions, for example rare-earth metal ions (especially La³⁺,particularly Tm³⁺, Yb³⁺ or Lu³⁺ (Chen et al. Biotechniques. 2002, 32:518-520; Komiyama et al. Chem. Commun. 1999, 1443-1451)), Fe(3) orCu(3), or exposure to elevated pH, e.g. treatment with a base such assodium hydroxide. By “selective cleavage of the phosphodiester bondbetween a deoxyribonucleotide and a ribonucleotide” is meant that thechemical cleavage agent is not capable of cleaving the phosphodiesterbond between two deoxyribonucleotides under the same conditions.

The base composition of the ribonucleotide(s) is generally not material,but can be selected in order to optimise chemical (or enzymatic)cleavage. By way of example, rUMP or rCMP may be used if cleavage is tobe carried out by exposure to metal ions, especially rare earth metalions.

The ribonucleotide(s) will typically be incorporated into one strand ofa template polynucleotide duplex (or the amplification primer from whichthis strand is derived if prepared by solid-phase amplification), andmay be situated in a region of the duplex which is single-stranded whenthe two complementary strands of the duplex are annealed (i.e. in a 5′overhanging portion). If the template polynucleotide duplex is preparedby solid-phase PCR amplification using forward and reverse amplificationprimers, one of which contains at least one ribonucleotide, the standardDNA polymerase enzymes used for PCR amplification are not capable ofcopying ribonucleotide templates. Hence, the PCR products will containan overhanging 5′ region comprising the ribonucleotide(s) and anyremainder of the amplification primer upstream of the ribonucleotide(s).

The phosphodiester bond between a ribonucleotide and adeoxyribonucleotide, or between two ribonucleotides may also be cleavedby an RNase. Any endolytic ribonuclease of appropriate substratespecificity can be used for this purpose. If the ribonucleotide(s) arepresent in a region which is single-stranded when the two complementarystrands of the double-stranded molecule are annealed (i.e. in a 5′overhanging portion), then the RNase will be an endonuclease which hasspecificity for single strands containing ribonucleotides. For cleavagewith ribonuclease, two or more consecutive ribonucleotides may beincluded in a particular embodiment, and more particularly from 2 to 10or from 5 to 10 consecutive ribonucleotides. The precise sequence of theribonucleotides is generally not material, except that certain RNaseshave specificity for cleavage after certain residues. Suitable RNasesinclude, for example, RNaseA, which cleaves after C and U residues.Hence, when cleaving with RNaseA the cleavage site must include at leastone ribonucleotide which is C or U.

Polynucleotides incorporating one or more ribonucleotides can be readilysynthesised using standard techniques for oligonucleotide chemicalsynthesis with appropriate ribonucleotide precursors. If the templatepolynucleotide duplex is prepared by solid-phase nucleic acidamplification, then it is convenient to incorporate one or moreribonucleotides into one of the primers to be used for the amplificationreaction.

iv) Photochemical Cleavage

The term “photochemical cleavage” encompasses any method which utiliseslight energy in order to achieve cleavage of one or both strands of thedouble-stranded nucleic acid molecule.

A site for photochemical cleavage can be provided by a non-nucleotidechemical spacer unit in one of the strands of the double-strandedmolecule (or the amplification primer from which this strand is derivedif prepared by solid-phase amplification). Suitable photochemicalcleavable spacers include the PC spacer phosphoamidite(4-(4,4′-Dimethoxytrityloxy)butyramidomethyl)-1-(2-nitrophenyl)-ethyl]-2-cyanoethyl-(N,N-diisopropyl)-phosphoramidite)supplied by Glen Research, Sterling, Va., USA (cat number 10-4913-XX)which has the structure:

The spacer unit can be cleaved by exposure to a UV light source.

This spacer unit can be attached to the 5′ end of a polynucleotide,together with a thiophosphate group which permits attachment to a solidsurface, using standard techniques for chemical synthesis ofoligonucleotides. Conveniently, this spacer unit can be incorporatedinto a forward or reverse amplification primer to be used for synthesisof a photocleavable template polynucleotide duplex by solid-phaseamplification.

v) Cleavage of Hemimethylated DNA

Site-specific cleavage of one strand of a double-stranded nucleic acidmolecule may also be achieved by incorporating one or more methylatednucleotides into this strand and then cleaving with an endonucleaseenzyme specific for a recognition sequence including the methylatednucleotide(s).

The methylated nucleotide(s) will typically be incorporated in a regionof one strand of the template polynucleotide duplex having acomplementary stretch of non-methylated deoxyribonucleotides on thecomplementary strand, such that annealing of the two strands produces ahemimethylated duplex structure. The hemimethylated duplex may then becleaved by the action of a suitable endonuclease. For the avoidance ofdoubt, enzymes which cleave such hemimethylated target sequences are notto be considered as “restriction endonucleases” excluded from the scopeof the second aspect of the invention, but rather are intended to formpart of the subject-matter of the invention.

Polynucleotides incorporating one or methylated nucleotides may beprepared using standard techniques for automated DNA synthesis, usingappropriately methylated nucleotide precursors. If the templatepolynucleotide duplex is prepared by solid-phase nucleic acidamplification, then it is convenient to incorporate one or moremethylated nucleotides into one of the primers to be used for theamplification reaction.

vi) PCR Stoppers

In another embodiment of the invention the template polynucleotideduplex may be prepared by solid-phase amplification using forward andreverse primers, one of which contains a “PCR stopper”. A “PCR stopper”is any moiety (nucleotide or non-nucleotide) which prevents read-throughof the polymerase used for amplification, such that it cannotextend/copy beyond that point. The result is that amplified strandsderived by extension of the primer containing the PCR stopper willcontain a 5′ overhanging portion. This 5′ overhang (other than the PCRstopper itself) may be comprised of naturally occurringdeoxyribonucleotides, with predominantly natural backbone linkages, i.e.it may simply be a stretch of single-stranded DNA. The molecule may thenbe cleaved in the 5′ overhanging region with the use of a cleavagereagent (e.g. an enzyme) which is selective for cleavage ofsingle-stranded DNA but not double stranded DNA, for example mung beannuclease.

The PCR stopper may be essentially any moiety which preventsread-through of the polymerase to be used for the amplificationreaction. Suitable PCR stoppers include, but are not limited to,hexaethylene glycol (HEG), abasic sites, and any non-natural or modifiednucleotide which prevents read-through of the polymerase, including DNAanalogues such as peptide nucleic acid (PNA).

Stable abasic sites can be introduced during chemical oligonucleotidesynthesis using appropriate spacer units containing the stable abasicsite. By way of example, abasic furan(5′-O-Dimethoxytrityl-1′,2′-Dideoxyribose-3′-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite)spacers commercially available from Glen Research, Sterling, Va., USA,can be incorporated during chemical oligonucleotide synthesis in orderto introduce an abasic site. Such a site can thus readily be introducedinto an oligonucleotide primer to be used in solid-phase amplification.If an abasic site is incorporated into either forward or reverseamplification primer the resulting amplification product will have a 5′overhang on one strand which will include the abasic site (insingle-stranded form). The single-stranded abasic site may then becleaved by the action of a suitable chemical agent (e.g. exposure toalkali) or an enzyme (e.g. AP-endonuclease VI, Shida et al. NucleicAcids Research, 1996, Vol. 24, 4572-4576).

vii) Cleavage of Peptide Linker

A cleavage site can also be introduced into one strand of a templatepolynucleotide duplex by preparing a conjugate structure in which apeptide molecule is linked to one strand of the duplex (or theamplification primer from which this strand is derived if prepared bysolid-phase amplification). The peptide molecule can subsequently becleaved by a peptidase enzyme of the appropriate specificity, or anyother suitable means of non-enzymatic chemical or photochemicalcleavage. Typically, the conjugate between peptide and nucleic acid willbe formed by covalently linking a peptide to one strand only of thetemplate polynucleotide duplex, with the peptide portion beingconjugated to the 5′ end of this strand, adjacent to the point ofattachment to the solid surface. If the template polynucleotide duplexis prepared by solid-phase amplification, the peptide conjugate may beincorporated at the 5′ end of one of the amplification primers.Obviously the peptide component of this primer will not be copied duringPCR amplification, hence the “bridged” amplification product willinclude a cleavable 5′ peptide “overhang” on one strand.

Conjugates between peptides and nucleic acids wherein the peptide isconjugated to the 5′ end of the nucleic acid can be prepared usingtechniques generally known in the art. In one such technique the peptideand nucleic acid components of the desired amino acid and nucleotidesequence can be synthesised separately, e.g. by standard automatedchemical synthesis techniques, and then conjugated in aqueous/organicsolution. By way of example, the OPeC™ system commercially availablefrom Glen Research is based on the “native ligation” of an N-terminalthioester-functionalized peptide to a 5′-cysteinyl oligonucleotide.Pentafluorophenyl S-benzylthiosuccinate is used in the final couplingstep in standard Fmoc-based solid-phase peptide assembly. Deprotectionwith trifluoroacetic acid generates, in solution, peptides substitutedwith an N-terminal S-benzylthiosuccinyl group.O-trans-4-(N-a-Fmoc-5-tert-butylsulfenyl-l-cysteinyl)aminocyclohexylO-2-cyanoethyl-N,N-diisopropylphosphoramidite is used in the finalcoupling step in standard phosphoramidite solid-phase oligonucleotideassembly. Deprotection with aqueous ammonia solution generates insolution 5′-S-tert-butylsulfenyl-L-cysteinyl functionalizedoligonucleotides. The thiobenzyl terminus of the Modified Peptide isconverted to the thiophenyl analogue by the use of thiophenol, whilstthe Modified Oligonucleotide is reduced usingtris(carboxyethyl)-phosphine. Coupling of these two intermediates,followed by the “native ligation” step, leads to formation of theOligonucleotide-Peptide Conjugate.

The conjugate strand containing peptide and nucleic acid can becovalently attached to a solid support using any suitable covalentlinkage technique known in the art which is compatible with the chosensurface. If the peptide/nucleic acid conjugate structure is anamplification primer to be used for solid-phase FOR amplification,attachment to the solid support must leave the 3′ end of the nucleicacid component free.

The peptide component can be designed to be cleavable by any chosenpeptidase enzyme, of which many are known in the art. The nature of thepeptidase is not particularly limited, it is necessary only for thepeptidase to cleave somewhere in the peptide component. Similarly, thelength and amino acid sequence of the peptide component is notparticularly limited except by the need to be “cleavable” by the chosenpeptidase.

The length and precise sequence of the nucleic acid component is alsonot particularly limited, it may be of any desired sequence. If thenucleic acid component is to function as a primer in solid-phase PCR,then its length and nucleotide sequence will be selected to enableannealing to the template to be amplified.

Enzymatic Digestion with Restriction Endonuclease/Nicking Endonuclease

Cleavage of double-stranded polynucleotides with restrictionendonuclease is a technique in routine use in the art of molecularbiology. Nicking endonucleases are enzymes that selectively cleave or“nick” one strand of a polynucleotide duplex and are also well known inthe art of molecular biology. The invention is not limited with respectto the nature of the enzyme. Essentially any restriction or nickingendonuclease may be used, provided that a suitable recognition sequencecan be included at the cleavage site.

The method of the invention is described in further detail as follows.

Any suitable solid support and any suitable attachment means known inthe art may be used, of which several are described by way of examplebelow. Linkage to the solid support may be achieved via covalentattachment.

The polynucleotide duplexes will typically be formed from twocomplementary polynucleotide strands comprised of deoxyribonucleotidesjoined by phosphodiester bonds, but may additionally include one or moreribonucleotides and/or non-nucleotide chemical moieties and/ornon-naturally occurring nucleotides and/or non-naturally occurringbackbone linkages. In particular, the double-stranded nucleic acid mayinclude non-nucleotide chemical moieties, e.g. linkers or spacers, atthe 5′ end of one or both strands. By way of non-limiting example, thedouble-stranded nucleic acid may include methylated nucleotides, uracilbases, phosphorothioate groups, ribonucleotides, diol linkages,disulphide linkages, peptides etc. Such non-DNA or non-naturalmodifications may be included in order to permit cleavage, or to confersome other desirable property, for example to enable covalent attachmentto a solid support, or to act as spacers to position a site of cleavagean optimal distance from the solid support.

The template duplexes may also include non-target sequences at both the5′ and 3′ ends, flanking the target polynucleotide. If the templateduplexes are formed by solid-phase amplification, these non-targetsequences will generally be derived from the primers used forsolid-phase amplification.

The polynucleotide duplexes form part of a single cluster or colonycomprised of many such first and second duplexes, and the cluster orcolony will itself typically form part of an array of many such clustersor colonies. The terms “cluster” and “colony” are used interchangeablythroughout and refer to a discrete site on a solid support comprised ofa plurality of identical immobilised nucleic acid strands and aplurality of identical immobilised complementary nucleic acid strands.The term “clustered array” refers to an array formed from such clustersor colonies.

A key feature of the invention is that both sequencing runs can occur inthe same cluster or colony on a clustered array. On such an array eachduplex within each colony will comprise the same double-stranded targetpolynucleotide, whereas different colonies may be formed of duplexescomprising different double-stranded target polynucleotides. In aparticular embodiment at least 90%, more particularly at least 95% ofthe colonies on a given clustered array will be formed from templateduplexes comprising different double-stranded target polynucleotides,although within each individual colony on the array all templateduplexes will comprise the same double-stranded target polynucleotide.

The amplified polynucleotides can then be treated in such a way to allowprimer hybridisation. This can be performed either by heating theamplified clusters to denature the duplexes, followed by cooling in thepresence of the first sequencing primer, by a chemical treatment such assodium hydroxide to denature the duplexes or by a treatment to cleaveone or both of the strands of the duplex polynucleotide.

Each polynucleotide duplex on the array contains the same universalprimer recognition regions to allow the same primers to be used tosequence every cluster. A first sequencing primer is then hybridised tothe first template strand and a sequencing reaction proceeds viasuccessive incorporation of nucleotides to the first sequencing primer,resulting in determination of the sequence of a first region of thetarget polynucleotide.

Hybridisation of sequencing primer to the template strand is achieved bycontacting the primer and template strand under conditions which promoteannealing of primer to template. Such conditions will generally be wellknown to those skilled in the art of molecular biology.

When the first sequencing reaction is complete, the extended firstsequencing primer is removed from the surface. This can be achieved byheating, or chemical denaturation. A second sequencing primer is thenhybridised to a second region of the template and a sequencing reactionproceeds via successive addition of nucleotides to the second sequencingprimer, resulting in determination of the sequence of a second region ofthe target polynucleotide.

Sequencing can be carried out using any suitable“sequencing-by-synthesis” technique, wherein nucleotides are addedsuccessively to a free 3′ hydroxyl group, typically provided byannealing of a sequencing primer, resulting in synthesis of apolynucleotide chain in the 5′ to 3′ direction. In a particularembodiment, the nature of the nucleotide added is determined after eachaddition.

One particular sequencing method which can be used in the methods of theinvention relies on the use of modified nucleotides that can act asreversible chain terminators. Nucleotides for use in the invention aredescribed fully in WO04018497 and U.S. Pat. No. 7,057,026. Once themodified nucleotide has been incorporated into the growingpolynucleotide chain complementary to the region of the template beingsequenced there is no free 3′-OH group available to direct furthersequence extension and therefore the polymerase can not add furthernucleotides. Once the nature of the base incorporated into the growingchain has been determined, the 3′ block may be removed to allow additionof the next successive nucleotide. By ordering the products derivedusing these modified nucleotides it is possible to deduce the DNAsequence of the DNA template. Such reactions can be done in a singleexperiment if each of the modified nucleotides has attached thereto adifferent label, known to correspond to the particular base, whichfacilitates discrimination between the bases added at each incorporationstep. Alternatively, a separate reaction may be carried out containingeach of the modified nucleotides, which are added separately.

The modified nucleotides may carry a label to facilitate theirdetection. In a particular embodiment, the label is a fluorescent label.Each nucleotide type may carry a different fluorescent label.Fluorescent labels suitable for use in the current invention aredescribed in U.S. application 60/801,270. However the detectable labelneed not be a fluorescent label. Any label can be used which allows thedetection of the incorporation of the nucleotide into the DNA sequence.

One method for detecting the fluorescently labelled nucleotidescomprises using laser light of a wavelength specific for the labellednucleotides, or the use of other suitable sources of illumination. Thefluorescence from the label on the nucleotide may be detected by a CCDcamera or other suitable detection means. An imaging system suitable fordetermining the fluorescent signal from incorporated nucleotides isdescribed in application No. 60/788,248.

The methods of the invention are not limited to use of the sequencingmethod outlined above, but can be used in conjunction with essentiallyany sequencing methodology which relies on successive incorporation ofnucleotides into a polynucleotide chain. Suitable techniques include,for example, Pyrosequencing™, FISSEQ (fluorescent in situ sequencing),MPSS (massively parallel signature sequencing) and sequencing byligation-based methods, for example as described in U.S. Pat. No.6,306,597.

The target double-stranded polynucleotide to be sequenced using themethod of the invention may be any polynucleotide that it is desired tosequence. The target polynucleotide may be of known, unknown orpartially known sequence, such as, for example in re-sequencingapplications. Using the template preparation method described in detailbelow it is possible to prepare arrays of templates starting fromessentially any double-stranded target polynucleotide of known, unknownor partially known sequence. With the use of arrays it is possible tosequence multiple targets of the same or different sequence in parallel.A particular application of the pairwise method is in the sequencing offragments of genomic DNA. The method provides particular advantages inthe identification of genome rearrangements, since the two regions ofsequence obtained for each target molecule using the method will beknown to be linked within a certain distance of each other in thegenome, depending on the size of the starting target molecule.

Preparation of Templates to be Sequenced

Suitable templates for sequencing using the method of the invention canbe prepared by solid-phase nucleic acid amplification to produce nucleicacid colonies. This can be done using procedures analogous to thosedescribed in WO 98/44151 and WO 00/18957, the contents of which areincorporated herein in their entirety by reference.

For amplification to proceed, a mixture of two amplification primers isimmobilised or “grafted” onto the surface of a suitable solid support.

The amplification primers are oligonucleotide molecules having thefollowing structures:

Forward primer: A-L-X—S1Reverse primer: A-L-Y—S2

Wherein A represents a moiety which allows attachment to the solidsupport, L is an optional linker moiety, X is an optional cleavage siteand S1 and S2 are polynucleotide sequences which permit amplification ofa template nucleic acid molecule comprising the target double-strandedpolynucleotide.

The mixture of primers will generally comprise substantially equalamounts the forward and reverse primers.

L represents a linker which may be included but is not strictlynecessary. The linker may be a carbon-containing chain such as those offormula (CH₂)_(n) wherein “n” is from 1 to about 1500, for example lessthan about 1000, particularly less than 100, e.g. from 2-50,particularly 5-25. However, a variety of other linkers may be employedwith the only restriction placed on their structures being that thelinkers are stable under conditions under which the polynucleotides areintended to be used subsequently, e.g. conditions used in DNAamplification and sequencing.

Linkers which do not consist of only carbon atoms may also be used. Suchlinkers include polyethylene glycol (PEG) having a general formula of(CH₂—CH₂—O)_(m), wherein m is from about 1 to 600, particularly lessthan about 500.

Linkers formed primarily from chains of carbon atoms and from PEG may bemodified so as to contain functional groups which interrupt the chains.Examples of such groups include ketones, esters, amines, amides, ethers,thioethers, sulfoxides, sulfones. Separately or in combination with thepresence of such functional groups may be employed alkene, alkyne,aromatic or heteroaromatic moieties, or cyclic aliphatic moieties (e.g.cyclohexyl). Cyclohexyl or phenyl rings may, for example, be connectedto a PEG or (CH₂)_(n) chain through their 1- and 4-positions.

As an alternative to the linkers described above, which are primarilybased on linear chains of saturated carbon atoms, optionally interruptedwith unsaturated carbon atoms or heteroatoms, other linkers may beenvisaged which are based on nucleic acids or monosaccharide units (e.g.dextrose). It is also within the scope of this invention to utilisepeptides as linkers.

In a further embodiment linker may comprise one or more nucleotideswhich form part of the amplification primer but which do not participatein any reaction carried out on or with the primer (e.g. a hybridisationor amplification reaction). Such nucleotides may also be referred toherein as “spacer” polynucleotides. Typically from 1 to 20, moreparticularly from 1 to 15 or from 1 to 10, and more particularly 2, 3,4, 5, 6, 7, 8, 9 or 10 spacer nucleotides may be included. Mostparticularly the primer will include 10 spacer nucleotides. PolyTspacers may be used, although other nucleotides and combinations thereofcan also be used. In one particular embodiment the primer may include10T spacer nucleotides.

The one or more spacer nucleotides function to space the portion of theprimer required to hybridise to a target and direct amplification, awayfrom the site of attachment to the solid support (i.e. S1 or S2). Theinclusion of spacer nucleotides at the 5′ end can markedly improve theperformance of hybridisation of complementary polynucleotides to regionS1 or S2. In a particular embodiment the polynucleotide will include 10Tspacer nucleotides and a 5′ phosphorothioate group for attachment to thesolid support (moiety A), although other attachment moieties may be usedas discussed below.

Sequences S1 and S2 in the forward and reverse primers arepolynucleotide sequences which, in combination, direct amplification ofa template by solid-phase bridging amplification reaction. The templateto be amplified must itself comprise (when viewed as a single strand) atthe 3′ end a sequence capable of hybridising to sequence S1 in theforward primers and at the 5′ end a sequence the complement of which iscapable of hybridising to sequence S2 the reverse primer.

The precise nature of sequences S1 and S2 in the forward and reverseprimer oligonucleotides will be dependent on the nature of the templateit is intended to amplify. S1 and S2 must be capable of hybridising tocognate sequences on complementary strands of the template to beamplified. The term “hybridisation” encompasses sequence-specificbinding between primer and template. Binding of a primer to its cognatesequence in the template should occur under typical conditions used forprimer-template annealing in standard PCR. Typically hybridisationconditions are 5×SSC at 40° C., following an initial denaturation step.It is not essential for hybridisation that sequences S1 and S2 beexactly complementary to their cognate sequences in the template to beamplified.

S1 and S2 may be of different or identical sequence and will typicallybe around 20-30 nucleotides in length. The primers can include naturaland non-natural DNA bases, also ribonucleotides or any combinationthereof, and may also include non-natural backbone linkages such asdisulphides or phosphorothioates.

Cleavage site X may fall within sequence S1 or S2, or if the linker L isitself a polynucleotide cleavage they may form part of linker region L.In other embodiments the cleavage site may be formed at the junction ofsequences L and S1 or L and S2, or at the junction between moiety A andlinker L (if present) or between moiety A and sequence S1 or S2 (if Lnot present).

Moiety A may be any chemical moiety which permits immobilisation of anoligonucleotide primer on a solid support. The surface of the solidsupport may itself be functionalised to permit attachment of theprimers. Any suitable covalent or non-covalent attachment means may beused, of which many are known in the art.

By way of example, biotinylated albumins (BSA) can form a stableattachment of biotin groups by physisorption of the protein ontosurfaces. Covalent modification can also be performed using silanes,which have been used to attach molecules to a solid support, usually aglass slide. By way of example, a mixture of tetraethoxysilane andtriethoxy-bromoacetamidopropyl-silane (e.g. in a ratio of 1:100) can beused to prepare functionalised glass slides which permit attachment ofmolecules nucleic acids including a thiophosphate or phosphorothioatefunctionality. Biotin molecules can be attached to surfaces usingappropriately reactive species such as biotin-PEG-succinimidyl esterwhich reacts with an amino surface. A mixture of amplification primersmay then be brought into contact with the functionalised solid support.

In alternative embodiments functionalised polyacrylamide hydrogels maybe used to attach primers wherein moiety A is a sulfur-containingnucleophilic groups are used. Examples of appropriate sulfurnucleophile-containing polynucleotides are disclosed in Zhao et al(Nucleic Acids Research, 2001, 29(4), 955-959) and Pirrung et al(Langmuir, 2000, 16, 2185-2191) and include, for example, simple thiols,thiophosphates and thiophosphoramidates. Particular hydrogels are thoseformed from a mixture of (i) a first comonomer which is acrylamide,methacrylamide, hydroxyethyl methacrylate or N-vinyl pyrrolidinone; and

(ii) a second comonomer which is a functionalised acrylamide or acrylateof formula (I):

H₂C═C(H)—C(═O)-A-B—C  (I);

or a methacrylate or methacrylamide of formula (II):

or H₂C═C(CH₃)—C(═O)-A-B—C—  (II)

(wherein:

A is NR or O, wherein R is hydrogen or an optionally substitutedsaturated hydrocarbyl group comprising 1 to 5 carbon atoms;

—B— is an optionally substituted alkylene biradical of formula—(CH₂)_(n)— wherein n is an integer from 1 to 50; and wherein n=2 ormore, one or more optionally substituted ethylene biradicals —CH₂CH₂— ofsaid alkylene biradical may be independently replaced by ethenylene andethynylene moieties; and wherein n=1 or more, one or more methylenebiradicals —CH₂— may be replaced independently with an optionallysubstituted mono- or polycyclic hydrocarbon biradical comprising from 4to 50 carbon atoms, or a corresponding heteromonocyclic orheteropolycyclic biradical wherein at least 1 CH₂ or CH₂ is substitutedby an oxygen sulfur or nitrogen atom or an NH group; and

C is a group for reaction with a compound to bind the compoundcovalently to the hydrogel) to form a polymerised product. A particularhydrogel is formed by co-polymerisation of acrylamide andN-(5-bromoacetamidylpentyl)acrylamide (BRAPA).

The term “solid support”, as used herein, refers to the material towhich the polynucleotides molecules are attached. Suitable solidsupports are available commercially, and will be apparent to the skilledperson. The supports can be manufactured from materials such as glass,ceramics, silica and silicon. Supports with a gold surface may also beused. The supports usually comprise a flat (planar) surface, or at leasta structure in which the polynucleotides to be interrogated are inapproximately the same plane. Alternatively, the solid support can benon-planar, e.g., a microbead. Any suitable size may be used. Forexample, the supports might be on the order of 1-10 cm in eachdirection.

For the grafting reaction to proceed a mixture of the amplificationprimers is applied to a (suitable functionalised) solid support underconditions which permit reaction between moiety A and the support. Theresult of the grafting reaction is a substantially even distribution ofthe primers over the solid support.

In certain embodiments the template to be amplified may be grafted ontothe solid support together with the amplification primers in a singlegrafting reaction. This can be achieved by adding template moleculesincluding moiety A at the 5′ end to the mixture of primers to form aprimer-template mixture. This mixture is then grafted onto the solidsupport in a single step. Amplification may then proceed using theimmobilised template and primers in a reaction analogous to thatdescribed in WO 00/18957. The first step in such a reaction will behybridisation between surface-bound templates and surface-boundamplification primers.

If the mixture of primers only is grafted onto the solid support and thetemplate to be amplified is present in free solution, the amplificationreaction may proceed substantially as described in WO 98/44151. Briefly,following attachment of the primers the solid support is contacted withthe template to be amplified under conditions which permit hybridisationbetween the template and the immobilised primers. The template isusually added in free solution under suitable hybridisation conditions,which will be apparent to the skilled reader. Typically hybridisationconditions are, for example, 5×SSC at 40° C., following an initialdenaturation step. Solid-phase amplification can then proceed, the firststep of the amplification being a primer extension step in whichnucleotides are added to the 3′ end of the immobilised primer hybridisedto the template to produce a fully extended complementary strand. Thiscomplementary strand will thus include at its 3′ end a sequence which iscapable of binding to the second primer molecule immobilised on thesolid support. Further rounds of amplification (analogous to a standardPCR reaction) lead to the formation of clusters or colonies of templatemolecules bound to the solid support.

Sequences S1 and S2 in the amplification primers may be specific for aparticular target nucleic acid that it is desired to amplify, but inother embodiments sequences S1 and S2 may be “universal” primersequences which enable amplification of any target nucleic acid of knownor unknown sequence which has been modified to enable amplification withthe universal primers.

Suitable templates to be amplified with universal primers may beprepared by modifying target double-stranded polynucleotides by additionof known adaptor sequences to the 5′ and 3′ ends of the target nucleicacid molecules to be amplified. The target molecules themselves may beany double-stranded molecules it is desired to sequence (e.g. randomfragments of human genomic DNA). The adaptor sequences enableamplification of these molecules on a solid support to form clustersusing forward and reverse primers having the general structure describedabove, wherein sequences S1 and S2 are universal primer sequences.

The adaptors are typically short oligonucleotides that may besynthesised by conventional means. The adaptors may be attached to the5′ and 3′ ends of target nucleic acid fragments by a variety of means(e.g. subcloning, ligation. etc). More specifically, two differentadaptor sequences are attached to a target nucleic acid molecule to beamplified such that one adaptor is attached at one end of the targetnucleic acid molecule and another adaptor is attached at the other endof the target nucleic acid molecule. The resultant construct comprisinga target nucleic acid sequence flanked by adaptors may be referred toherein as a “template nucleic acid construct”.

The target double-stranded polynucleotides may advantageously besize-fractionated prior to modification with the adaptor sequences.

The adaptors contain sequences which permit nucleic acid amplificationusing the amplification primer molecules immobilised on the solidsupport. These sequences in the adaptors may be referred to herein as“primer binding sequences”. In order to act as a template for nucleicacid amplification, a single strand of the template construct mustcontain a sequence which is complementary to sequence S1 in the forwardamplification primers (such that the forward primer molecule can bindand prime synthesis of a complementary strand) and a sequence whichcorresponds to sequence S2 in the reverse amplification primer molecules(such that the reverse primer molecule can bind to the complementarystrand). The sequences in the adaptors which permit hybridisation toprimer molecules will typically be around 20-30 nucleotides in length,although the invention is not limited to sequences of this length.

The precise identity of sequences S1 and S2 in the amplificationprimers, and hence the cognate sequences in the adaptors, are generallynot material to the invention, as long as the primer molecules are ableto interact with the amplification sequences in order to direct bridgingamplification. The criteria for design of primers are generally wellknown to those of ordinary skill in the art.

Solid-phase amplification by either the method analogous to that of WO98/44151 or that of WO 00/18957 will result in production of an array ofcolonies of “bridged” amplification products. Both strands of theamplification product will be immobilised on the solid support at ornear the 5′ end, this attachment being derived from the originalattachment of the amplification primers. Typically the amplificationproducts within each colony will be derived from amplification of asingle target molecule.

The utility of the sequencing method of the invention is not limited tosequencing of templates produced by an amplification reaction. Themethod may be applied to sequencing of double-stranded templatesimmobilised on a support by any other means amenable to repeated cyclesof hybridisation and sequencing.

The invention will be further understood with reference to the followingexperimental examples:

EXAMPLES

The following are examples of general techniques which may be applied incarrying out the method of the invention. Clusters can be made asdescribed in published reference WO07010251, the protocols of which areincorporated herein by reference.

Example 1 Acrylamide Coating of Glass Chips

The solid supports used are typically 8-channel glass chips such asthose provided by Silex Microsystems (Silex Microsystems, Sweden),Micronit (Twente, Nederland) or IMT (Neuchâtel, Switzerland). However,the experimental conditions and procedures are readily applicable toother solid supports.

Chips were washed as follows: neat Decon for 30 min, milliQ H₂O for 30min, NaOH 1N for 15 min, milliQ H₂O for 30 min, HCl 0.1N for 15 min,milliQ H₂O for 30 min.

Polymer Solution Preparation

For 10 ml of 2% polymerisation mix.

-   -   10 ml of 2% solution of acrylamide in milliQ H2O    -   165 μl of a 100 mg/ml N-(5-bromoacetamidylpentyl) acrylamide        (BRAPA) solution in DMF (23.5 mg in 235 μl DMF)    -   11.5 μl of TEMED    -   100 μl of a 50 mg/ml solution of potassium persulfate in milliQ        H₂O (20 mg in 400 μl H₂O)

The 10 ml solution of acrylamide was first degassed with argon for 15min. The solutions of BRAPA, TEMED and potassium persulfate weresuccessively added to the acrylamide solution. The mixture was thenquickly vortexed and used immediately. Polymerization was then carriedout for 1 h 30 at RT. Afterwards the channels were washed with milliQH₂O for 30 min. The slide was then dried by flushing argon through theinlets and stored under low pressure in a desiccator.

Example 2 Synthesis of N-(5-bromoacetamidylpentyl) acrylamide (BRAPA)

N-Boc-1,5-diaminopentane toluene sulfonic acid was obtained fromNovabiochem. The bromoacetyl chloride and acryloyl chloride wereobtained from Fluka. All other reagents were Aldrich products.

To a stirred suspension of N-Boc-1,5-diaminopentane toluene sulfonicacid (5.2 g, 13.88 mmol) and triethylamine (4.83 ml, 2.5 eq) in THF (120ml) at 0° C. was added acryloyl chloride (1.13 ml, 1 eq) through apressure equalized dropping funnel over a one hour period. The reactionmixture was then stirred at room temperature and the progress of thereaction checked by TLC (petroleum ether:ethyl acetate 1:1). After twohours, the salts formed during the reaction were filtered off and thefiltrate evaporated to dryness. The residue was purified by flashchromatography (neat petroleum ether followed by a gradient of ethylacetate up to 60%) to yield 2.56 g (9.98 mmol, 71%) of product 2 as abeige solid. ¹H NMR (400 MHz, d₆-DMSO): 1.20-1.22 (m, 2H, CH₂),1.29-1.43 (m, 13H, tBu, 2×CH₂), 2.86 (q, 2H, J=6.8 Hz and 12.9 Hz, CH₂),3.07 (q, 2H, J=6.8 Hz and 12.9 Hz, CH₂), 5.53 (dd, 1H, J=2.3 Hz and 10.1Hz, CH), 6.05 (dd, 1H, J=2.3 Hz and 17.2 Hz, CH), 6.20 (dd, 1H, J=10.1Hz and 17.2 Hz, CH), 6.77 (t, 1H, J=5.3 Hz, NH), 8.04 (bs, 1H, NH). Mass(electrospray+) calculated for C₁₃H₂₄N₂O₃ 256. found 279 (256+Na⁺).

Product 2 (2.56 g, 10 mmol) was dissolved in trifluoroaceticacid:dichloromethane (1:9, 100 ml) and stirred at room temperature. Theprogress of the reaction was monitored by TLC (dichloromethane:methanol9:1). On completion, the reaction mixture was evaporated to dryness, theresidue co-evaporated three times with toluene and then purified byflash chromatography (neat dichloromethane followed by a gradient ofmethanol up to 20%). Product 3 was obtained as a white powder (2.43 g, 9mmol, 90%). ¹H NMR (400 MHz, D₂O): 1.29-1.40 (m, 2H, CH₂), 1.52 (quint.,2H, j=7.1 Hz, CH₂), 1.61 (quint., 2H, J=7.7 Hz, CH₂), 2.92 (t, 2H, J=7.6Hz, CH₂), 3.21 (t, 2H, J=6.8 Hz, CH₂), 5.68 (dd, 1H, J=1.5 Hz and 10.1Hz, CH), 6.10 (dd, 1H, J=1.5 Hz and 17.2 Hz, CH), 6.20 (dd, 1H, J=10.1Hz and 17.2 Hz, CH). Mass (electrospray+) calculated for C₈H₁₆N₂O 156.found 179 (156+Na⁺).

To a suspension of product 3 (6.12 g, 22.64 mmol) and triethylamine(6.94 ml, 2.2 eq) in THF (120 ml) was added bromoacetyl chloride (2.07ml, 1.1 eq), through a pressure equalized dropping funnel, over a onehour period and at −60° C. (cardice and isopropanol bath in a dewar).The reaction mixture was then stirred at room temperature overnight andthe completion of the reaction was checked by TLC(dichloromethane:methanol 9:1) the following day. The salts formedduring the reaction were filtered off and the reaction mixtureevaporated to dryness. The residue was purified by chromatography (neatdichloromethane followed by a gradient of methanol up to 5%). 3.2 g(11.55 mmol, 51%) of the product 1 (BRAPA) were obtained as a whitepowder. A further recrystallization performed in petroleum ether:ethylacetate gave 3 g of the product 1. ¹H NMR (400 MHz, d₆-DMSO):1.21-1.30(m, 2H, CH₂), 1.34-1.48 (m, 4H, 2×CH₂), 3.02-3.12 (m, 4H, 2×CH₂), 3.81(s, 2H, CH₂), 5.56 (d, 1H, J=9.85 Hz, CH), 6.07 (d, 1H, J=16.9 Hz, CH),6.20 (dd, 1H, J=10.1 Hz and 16.9 Hz, CH), 8.07 (bs, 1H, NH), 8.27 (bs,1H, NH). Mass (electrospray+) calculated for C₁₀H₁₇BrN₂O₂ 276 or 278.found 279 (278+H⁺), 299 (276+Na⁺).

Example 3 Grafting of Primers

An SFA coated flowcell is placed onto a modified MJ-Researchthermocycler and attached to a peristaltic pump. Grafting mix consistingof 0.5 μM of a forward primer and 0.5 μM of a reverse primer in 10 mMphosphate buffer (pH 7.0) is pumped into the channels of the flowcell ata flow rate of 60 μl/min for 75 s at 20° C. The thermocycler is thenheated to 51.6° C., and the flowcell is incubated at this temperaturefor 1 hour. During this time, the grafting mix undergoes 18 cycles ofpumping: grafting mix is pumped in at 15 μl/min for 20 s, then thesolution is pumped back and forth (5 s forward at 15 μl/min, then 5 sbackward at 15 μl/min) for 180 s. After 18 cycles of pumping, theflowcell is washed by pumping in 5×SSC/5 mM EDTA at 15 μl/min for 300 sat 51.6° C. The thermocycler is then cooled to 20° C.

The primers are typically 5′-phosphorothioate oligonucleotidesincorporating any specific sequences or modifications required forcleavage. Their sequences and suppliers vary according to the experimentfor which they are used, and in this case are complementary to the5′-ends of the template duplex. For the experiment described, theamplified clusters contained a diol linkage in one of the graftedprimers. Diol linkages can be introduced by including a suitablephosphoramidite intermediate into one of the primers used forsolid-phase amplification, for example, as described in WO07010251.

The grafted primers contain a sequence of T bases at the 5′-end to actas a spacer group to aid linearisation and hybridization.Oligonucleotides were prepared using the diol phosphoramidite usingstandard coupling conditions on a commercial DNA synthesiser. The finalcleavage/deprotection step in ammonia cleaves the acetate groups fromthe protected diol moiety, so that the oligonucleotide in solutioncontains the diol modification. The sequences of the two primers graftedto the flowcell are:

P5 = 5′-PS-TTTTTTTTTT-Diol-AATGATACGGCGACCACCGA-3′ And P7 =5′-PS-TTTTTTTTTTCAAGCAGAAGACGGCATACGA-3′

Example 4 Cluster Formation

The DNA sequence used in the amplification process is a mixture of fivesingle monotemplate sequences, with ends complementary to the graftedprimers. The full sequence of one of the monotemplate duplexes is shownin FIG. 12, and the sequences or the 19 base variable target region isshown in FIG. 2. The duplex DNA (1 nM) is denatured using 0.1 M sodiumhydroxide treatment followed by snap dilution to the desired 0.2-2 pM‘working concentration’ in ‘hybridization buffer’ (5×SSC/0.1% Tween).

Surface amplification was carried out by thermocycling using an MJResearch thermocycler, coupled with an 8-way peristaltic pump IsmatecIPC ISM931 equipped with Ismatec tubing (orange/yellow, 0.51 mm ID).

The single stranded template is hybridised to the grafted primersimmediately prior to the amplification reaction, which thus begins withan initial primer extension step rather than template denaturation. Thehybridization procedure begins with a heating step in a stringent bufferto ensure complete denaturation prior to hybridisation. After thehybridization, which occurs during a 20 min slow cooling step, theflowcell was washed for 5 minutes with a wash buffer (0.3×SSC/0.1%Tween).

A typical amplification process is detailed in the following table,detailing the flow volumes per channel:

Flow Pumped T Time rate V Step Description (° C.) (sec) (μl/min) (μl) 1Pump Hybridization 20 120 60 120 pre-mix 2 Pump Hybridization 98.5 30015 75 mix 3 Remove bubbles 98.5 10 100  16.7 4 Stop flow and 98.5 30static 0 hold T 5 Slow cooling 98.5-40.2 19.5 min static 0 6 Pump washbuffer 40.2 300 15 75 7 Pump amplification 40.2 200 15 50 pre-mix 8 Pumpamplification 40.2 75 60 75 mix 9 First Extension 74 90 static 0 10 Denaturation 98.5 45 static 0 amp Re-fill channels 98.5 10 60 10 cyclesAnnealing 58 90 static 0 1 to 30 Extension 74 90 static 0 11  Hold at20° C. 20 for ever static 0 12  Pump wash buffer 74 300 15 75

Hybridisation pre mix (buffer)=5×SSC/0.1% Tween

Hybridisation mix=0.1 M hydroxide DNA sample, diluted in hybridisationpre mix

Wash buffer=0.3×SSC/0.1% Tween

Amplification pre mix=2 M betaine, 20 mM Tris, 10 mM Ammonium Sulfate, 2mM Magnesium sulfate, 0.1% Triton, 1.3% DMSO, pH 8.8

Amplification mix=2 M betaine, 20 mM Tris, 10 mM Ammonium Sulfate, 2 mMMagnesium sulfate, 0.1% Triton, 1.3% DMSO, pH 8.8 plus 200 μM dNTP mixand 25 units/mL of Taq polymerase (NEB Product ref M0273L)

The clusters can be treated in a number of ways to allow sequencing:

Example 5 Sequencing of Non-Linearised Clusters

All channels were then denatured by pumping through 0.1M NaOH for 5minutes at 15 microlitres/minute. To aid strand separation, the chipcontaining NaOH was heated to 80 degrees C., and sequencing primer inhybridisation buffer (0.3×SSC) was flushed in for 5 minutes at 15microlitres/minute. The chip was then cooled to 66 degrees C. andincubated at this temperature for 15 minutes.

The chip was cooled to 40 degrees C., and washed for 5 minutes in0.1×SSC/0.1% Tween.

Cycles of sequencing enzymology were performed as described below,showing incorporation on non-linearised clusters as well as linearisedclusters. Analysis of these images has revealed the extent ofincorporation on the non-linearised clusters to be about half that oflinearised clusters.

Following denaturation with 0.1 M NaOH, a second sequencing primer washybridised to give a second sequencing run from the other strand of thetemplate.

Example 6 Sequencing of Linearised Clusters Using Two HybridisationSteps onto a Single Stranded Template Step 1: Linearisation

To linearize the nucleic acid clusters formed within the flow cellchannels, the linearization buffer is flowed through the flow cell for20 mins at room temp at 15 μL/min (total volume=300 μL per channel),followed by water for 5 mins at r.t.

The linearisation buffer consists of 1429 μL of water, 64 mg of sodiumperiodate, 1500 μL of formamide, 60 μL of 1 M Tris pH 8, and 11.4 μL of3-aminopropanol, mixed for a final volume of 3 mL. The periodate isfirst mixed with the water while the Tris is mixed with the formamide.The two solutions are then mixed together and the 3-aminopropanol isadded to that mixture.

Step 2: Blocking Extendable 3′-OH Groups

To prepare the blocking pre-mix, 1360 μL of water, 170 μL of 10×blocking buffer (NEB buffer 4; product number B7004S), and, 170 μL ofcobalt chloride (25 mM) are mixed for a final volume of 1700 μL. Toprepare the blocking mix, 1065.13 μL of blocking pre-mix, 21.12 μL of125 μM ddNTP mix, and 13.75 μL of TdT terminal transferase (NEB; part noM0252S) are mixed to a final volume of 1100 μL.

To block the nucleic acid within the clusters formed in the flow cellchannels, the blocking buffer is flowed through the flow cell, and thetemperature is adjusted as shown in the exemplary embodiments below.

Flow Pumped T Time rate V Step Description (° C.) (sec) (μl/min) (μl) 1Pump Blocking 20 200 15 50 pre-mix 2 Pump Blocking mix 37.7 300 15 75 3Stop flow and 37.7 20 static 0 hold T 4 Cyclic pump 37.7 8 × 15/ 45Blocking mix and (20 + 180) static wait 5 Pump wash buffer 20 300 15 75

Step 3: Denaturation and Hybridization of Sequencing Primer

To prepare the primer mix, 895.5 μL of hybridization pre-mix/buffer and4.5 μl of sequencing primer (100 μM) are mixed to a final volume of 900μL. The sequences of the two sequencing primers used in these reactionsare as follows:

Seq primer for first read: 5′ AATGATACGGCGACCACCGAGATGAAGGTATAGATSeq primer for second read: 5′ ACACTCTTTCCCTACACGACGCTCTTCCGATC

To denature the nucleic acid within the clusters and to hybridize thesequencing primer, the appropriate solutions are flowed through the flowcell as described below:

Flow Pumped T Time rate V Step Description (° C.) (sec) (μl/min) (μl) 1Pump 0.1M NaOH 20 300 15 75 2 Pump TE 20 300 15 75 3 Pump Primer mix 20300 15 75 4 Hold at 60 C. 60 900 0 0 5 Pump wash buffer 40.2 300 15 75

After the first sequencing run, this process can be repeated to removethe first run and hybridise the second sequencing primer. Afterdenaturation and hybridization of the sequencing primer, the flowcell isready for sequencing.

Example 7 DNA Sequencing Cycles

Sequencing was carried out using modified nucleotides prepared asdescribed in International patent application WO 2004/018493, andlabelled with four different commercially available fluorophores(Molecular Probes Inc.).

A mutant 9° N polymerase enzyme (an exo-variant including the triplemutation L408Y/Y409A/P410V and C223S) was used for the nucleotideincorporation steps.

Incorporation mix, Incorporation buffer (50 mM Tris-HCl pH 8.0, 6 mMMgSO4, 1 mM EDTA, 0.05% (v/v) Tween −20, 50 mM NaCl) plus 110 nM YAVexo-C223S, and 1 μM each of the four labelled modified nucleotides, wasapplied to the clustered templates, and heated to 45° C.

Templates were maintained at 45° C. for 30 min, cooled to 20° C. andwashed with Incorporation buffer, then with 5×SSC/0.05% Tween 20.Templates were then exposed to Imaging buffer (100 mM Tris pH 7.0, 30 mMNaCl, 0.05% Tween 20, 50 mM sodium ascorbate, freshly dissolved).

Templates were scanned in 4 colours at room temp.

Templates were then exposed to sequencing cycles of Cleavage andIncorporation as follows:

Cleavage

Prime with Cleavage buffer (0.1 M Tris pH 7.4, 0.1 M NaCl and 0.05%Tween 20). Heat to 60° C.

Treat the clusters with Cleavage mix (100 mM TCEP in Cleavage buffer).

Wait for a total of 15 min in addition to pumping fresh buffer every 4min.

Cool to 20° C.

Wash with Enzymology buffer.

Wash with 5×SSC/0.05% Tween 20.

Prime with Imaging buffer.

Scan in 4 colours at RT.

Incorporation

Prime with Incorporation buffer Heat to 60° C.

Treat with Incorporation mix. Wait for a total of 15 min in addition topumping fresh Incorporation mix every 4 min.

Cool to 20° C.

Wash with Incorporation buffer.

Wash with 5×SSC/0.05% Tween 20.

Prime with imaging buffer.

Scan in 4 colours at RT.

Repeat the process of Incorporation and Cleavage for as many cycles asrequired.

Incorporated nucleotides were detected using a total internal reflectionbased fluorescent CCD imaging apparatus.

A schematic representation of the method of the present invention isshown in FIG. 1. Data from sequencing reactions is shown in FIGS. 2 and3. The sequencing data from each run was of comparable quality, and >99%of the clusters from the first run also generated sequencing data fromthe second run. Moreover, each of the sequences from the second runcould be aligned against one of the five expected sequences from thelibrary. This data clearly shows that it is possible to hybridise afirst sequencing primer to a linearised cluster, obtain a sequencingread, remove the first extended primer, hybridise a second primer andobtain a second read. Although the data shown was obtained on a mixtureof single templates of known sequence to verify that the method waseffective, the sequence of the template is not material to theeffectiveness of the invention, and therefore any template or 3′- and 5′modified library of templates prepared and amplified using the methodsdescribed herein falls within the scope of the invention.

1.-26. (canceled)
 27. A method for paired-end sequencing of a targetpolynucleotide comprising the steps of: (a) providing a targetpolynucleotide attached to a support comprising first and secondtemplate strands, wherein the first and second template strands comprisefirst and second regions, respectively, to be sequenced; (b) performinga first sequencing reaction, wherein nucleotides are sequentially addedto a first sequencing primer hybridized to the first template strand todetermine the sequence of the first region; (c) separating the firstregion from the first sequencing primer after the sequencing reaction ofstep (b); and (d) performing a second sequencing reaction, whereinnucleotides are sequentially added to a second sequencing primerhybridized to the second template strand to determine the sequence ofthe second region.
 28. The method of claim 27, wherein the first andsecond template strands are attached to the support at their 5′ ends.29. The method of claim 27, wherein the separating comprises removingthe first region from the support.
 30. The method of claim 29, whereinthe first region is removed by cleavage.
 31. The method of claim 30,wherein the cleavage comprises enzymatic cleavage.
 32. The method ofclaim 31, wherein the enzymatic cleavage comprises nicking the firsttemplate strand.
 33. The method of claim 30, wherein the cleavagecomprises chemical cleavage.
 34. The method of claim 27, wherein thefirst and second sequencing primers comprise different sequences. 35.The method of claim 27, wherein the nucleotides are labeled.
 36. Themethod of claim 27, wherein the nucleotides are fluorescently labeled.37. The method of claim 35, wherein each nucleotide comprises adifferent label.
 38. The method of claim 27, wherein the nature of thenucleotide is determined after each addition.
 39. The method of claim27, wherein the support is a planar support.
 40. The method of claim 27,wherein the sequencing is pyrosequencing.
 41. The method of claim 27,wherein the sequencing is sequencing-by-synthesis.
 42. The method ofclaim 27, wherein the second sequencing primer is attached to a support.43. The method of claim 27, wherein the target polynucleotide is afragment of genomic DNA.
 44. The method of claim 27, wherein bothstrands of the target polynucleotide remain attached to the support. 45.The method of claim 27, further comprising, prior to step (a),fragmenting a nucleic acid molecule to produce a fragment, wherein thefragment is the target polynucleotide.
 46. The method of claim 45,further comprising treating the fragment to repair the fragment ends.47. The method of claim 45, further comprising treating the fragment toadd a single nucleotide to the ends of the fragment.
 48. The method ofclaim 47, wherein the single nucleotide is added to the 3′ ends of thefragment.
 49. The method of claim 1, further comprising, prior to step(a), adding a linker to the target polynucleotide.
 50. The method ofclaim 49, wherein the linker comprises one or more nucleotides.
 51. Themethod of claim 49, wherein the linker comprises a primer site.
 52. Themethod of claim 49, wherein the linker comprises a cleavage site. 53.The method of claim 52, wherein the linker comprises a primer site andthe cleavage site is located before the primer site.
 54. The method ofclaim 53, wherein the primer site is the same sequence.
 55. The methodof claim 27, wherein the target polynucleotide comprises non-targetsequences at both 5′ and 3′ ends.
 56. The method of claim 27, furthercomprising, prior to step (a), modifying the target polynucleotide toadd adaptor sequences to the 5′ and 3′ ends of the targetpolynucleotide.
 57. The method of claim 56, wherein one adaptor isattached at one end of the target polynucleotide and a different adaptoris attached to the other end of the target polynucleotide.
 58. Themethod of claim 56, wherein the adaptors comprise primer bindingsequences.